Product NDC: | 68776-1005 |
Proprietary Name: | WYANDOTTE SANIFECT FOAM-E II |
Non Proprietary Name: | CHLOROXYLENOL |
Active Ingredient(s): | 2081980 mg/208198mL & nbsp; CHLOROXYLENOL |
Administration Route(s): | TOPICAL |
Dosage Form(s): | LIQUID |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 68776-1005 |
Labeler Name: | Alex C. Fergusson, Inc. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part333A |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20090106 |
Package NDC: | 68776-1005-1 |
Package Description: | 3785.41 mL in 1 JUG (68776-1005-1) |
NDC Code | 68776-1005-1 |
Proprietary Name | WYANDOTTE SANIFECT FOAM-E II |
Package Description | 3785.41 mL in 1 JUG (68776-1005-1) |
Product NDC | 68776-1005 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | CHLOROXYLENOL |
Dosage Form Name | LIQUID |
Route Name | TOPICAL |
Start Marketing Date | 20090106 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | Alex C. Fergusson, Inc. |
Substance Name | CHLOROXYLENOL |
Strength Number | 2081980 |
Strength Unit | mg/208198mL |
Pharmaceutical Classes |